| Project/Area Number |
15310149
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Living organism molecular science
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| Research Institution | Osaka University |
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Principal Investigator |
FUKASE Koichi Osaka University, Graduate School of Science, Professor, 大学院・理学研究科, 教授 (80192722)
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| Co-Investigator(Kenkyū-buntansha) |
FUJIMOTO Yukari Osaka University, Graduate School of Science, Assistant Professor, 大学院・理学研究科, 助手 (00362616)
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| Project Period (FY) |
2003 – 2004
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| Project Status |
Completed (Fiscal Year 2004)
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| Budget Amount *help |
¥15,800,000 (Direct Cost: ¥15,800,000)
Fiscal Year 2004: ¥6,200,000 (Direct Cost: ¥6,200,000)
Fiscal Year 2003: ¥9,600,000 (Direct Cost: ¥9,600,000)
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| Keywords | oligosaccharide / solid-phase synthesis / high throughput synthesis / affinity separation / stereoselective glycosylation / protective group / glycoconjugate / immunostimulation / 固相-液相ハイブリッド合成 / 糖鎖合成 / グリコシル化 / マンノシル化 / ペプチドグリカン / リピドA |
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| Research Abstract |
Efficient synthesis of oligosaccharides by using solid-phase method and hybrid method of solid-phase and liquid-phase was investigated. We previously established "Chemical Fishing" method, where desired compound having azide function is selectively fished out of the reaction mixture by using the specific reaction between solid-supported phosphine and azide. This method was applied to the solid-phase synthesis of the elicitor pentasaccharide. Synthetic study of N-linked oligosaccharide of glycoprotein was also investigated. We developed a novel method for cleavage of trichloroethoxycarbonyl(Troc) group by radical reaction using (Bu_3Sn)_2. This method was then applied to solid-phase synthesis and rendered the use of Troc group for stereocontrolled β-glucosaminilation on solid-support by using its neighboring group participation effect. Stereoselective β-mannosylation was effected by using 4,6-O-benzylidene mannnosyl N-phenyltrifluoroacetimidate as a glycosyl donor and TMSOTf as an acid catalyst(α:β=1:9). We also established α-selective sialylation by using N-phthaloyl sialic acid phenyltrifluoroacetimidate as a donor and TMSOTf as an acid catalyst.
We previously reported Synthesis based on affinity separation(SAS), where desired compound having a tag moiety is rapidly separated from a reaction mixture by using specific affinity between the tag and the molecule that recognizes the tag. In the present study, we developed the new SAS method using the interaction between podand ether tag and solid-supported ammonium ion. The present method was applied to the rapid synthesis of small oligosaccharide library including Lewis X. Various partial structures and analogues of immunostimulating glycoconjugate lipopolysaccharide and peptidoglycan were synthesized in order to elucidate their biological functions.
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